Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K884588 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Heliomolar Refill 20x0.25g 110/A1, Product code 541501AN, Catalog number 541501 | 3 | 02/21/2018 | Ivoclar Vivadent, Inc. |
Heliomolar Refill 20x0.25g 110T, Product code 550559AN, Catalog number 550559 | 3 | 02/21/2018 | Ivoclar Vivadent, Inc. |
Heliomolar Refill 20x0.25g 140/A2, Product code 541502AN, Catalog number 541502 | 3 | 02/21/2018 | Ivoclar Vivadent, Inc. |
Heliomolar Refill 20x0.25g 210/A3, Product code 541503AN, Catalog number 541503 | 3 | 02/21/2018 | Ivoclar Vivadent, Inc. |
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